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Cyclohexanecarbonyl chloride → HCID 13423464, 화합물

HRID 2164451
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HRID 2164451 반응식
[NH2:1][C:2]1[O:3][N:4]=[C:5]2[C:10]=1[C:9](=[O:11])[N:8]([CH3:12])[C:7](=[O:13])[N:6]2[CH3:14].[CH:15]1([C:21](Cl)=[O:22])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1>N1C=CC=CC=1>[CH:15]1([C:21]([NH:1][C:2]2[O:3][N:4]=[C:5]3[C:10]=2[C:9](=[O:11])[N:8]([CH3:12])[C:7](=[O:13])[N:6]3[CH3:14])=[O:22])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1
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참가 물질

4

반응물 2

HCID 75938Cyclohexanecarbonyl chlorideHCID 126779883-Amino-5,7-dimethyl[1,2]oxazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione

생성물 1

HCID 13423464HCID 13423464, 화합물수율 57.5%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
50 °C

실험 절차

To a solution of 17.5 g of 3-amino-5,7-dimethylisoxazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione in 350 ml of pyridine, 26.2 g of cyclohexanecarbonyl chloride was added and the mixture was heated at 50° C. for 3 hours. The mixture was evaporated to dryness under reduced pressure and 200 ml of methanol was added to the residue. The resultant crystals were recrystallized twice from chloroform-methanol to afford 15.7 g of colorless needles, m.p. 210°-212° C.

후처리

  1. customThe mixture was evaporated to dryness under reduced pressure and 200 ml of methanol
  2. additionwas added to the residue
  3. customThe resultant crystals were recrystallized twice from chloroform-methanol

출처 및 근거

ORD 기록
ord-46a4e32957ff44e59b2294eff29dfaee
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04504662

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